skip to main content

زبان محتوا

پشتیبانی: CRM@email.irandoc.ac.ir

Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Dominant hereditary disorder, NOS > Autosomal dominant congenital fibre-type disproportion myopathy due to selenoprotein N mutation
... > Clinical finding (finding) > disease > Genetic disease > Congenital myopathy with fibre type disproportion > Congenital fiber-type disproportion myopathy due to SELENON mutation > Autosomal dominant congenital fibre-type disproportion myopathy due to selenoprotein N mutation

اصطلاح مرجح

Autosomal dominant congenital fibre-type disproportion myopathy due to selenoprotein N mutation  

نوع

  • http://www.irandoc.ac.ir/onto/irandoc-meta/Concept

مورفولوژی مرتبط

محل یافتن

وقوع

فرآیند پاتولوژیک

URI

http://www.irandoc.acir/onto/irandoc/1202024009

این مفهوم را بارگیری کن: